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VFEND®Principal Display Panel (voriconazole)

PRINCIPAL DISPLAY PANEL - 50 mg Tablet Bottle Label

Pfizer

NDC 0049-3170-30

Vfend®
(voriconazole)

50 mg

Tablets

30 Tablets
Rx only

PRINCIPAL DISPLAY PANEL - 50 mg Tablet Bottle Label

PRINCIPAL DISPLAY PANEL - 200 mg Tablet Bottle Label

Pfizer

NDC 0049-3180-30

Vfend®
(voriconazole)

200 mg

Tablets

30 Tablets
Rx only

PRINCIPAL DISPLAY PANEL - 200 mg Tablet Bottle Label

PRINCIPAL DISPLAY PANEL - 200 mg Vial Label

NDC 0049-3190-28

Vfend® I.V.
(voriconazole) for injection
200 mg*
200 mg* of voriconazole

Not made with natural rubber latex
No Preservatives

Sterile Single-Dose Vial - Discard
Unused Portion
For Intravenous Infusion Only

Pfizer
Hospital

Rx only

PRINCIPAL DISPLAY PANEL - 200 mg Vial Label

PRINCIPAL DISPLAY PANEL - 200 mg Vial Carton

NDC 0049-3190-28
Rx only

1 Vial
Vfend® I.V.
(voriconazole) for injection

200 mg*
200 mg* of voriconazole

Not made with natural
rubber latex
No Preservatives

Sterile Single-Dose Vial -
Discard Unused Portion

For Intravenous Infusion Only

Pfizer
Hospital

PRINCIPAL DISPLAY PANEL - 200 mg Vial Carton

PRINCIPAL DISPLAY PANEL - 40 mg Bottle Label

Pfizer
NDC 0049-3160-44

Vfend®
(voriconazole)
for oral suspension

40 mg/mL*

ORANGE FLAVORED

75 mL (when reconstituted)

Rx only

PRINCIPAL DISPLAY PANEL - 40 mg Bottle Label

PRINCIPAL DISPLAY PANEL - 40 mg Bottle Carton

Pfizer
NDC 0049-3160-44

Vfend®
(voriconazole)
for oral suspension
40 mg/mL*

ORANGE FLAVORED

Oral Dispenser Included

Important: Read assembly instructions
carefully before dispensing.
Contains Small Parts -
Keep out of reach of children.

75 mL (when reconstituted)

Rx only

PRINCIPAL DISPLAY PANEL - 40 mg Bottle Carton
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Report Adverse Event
Pfizer Safety

To report an adverse event related to Pfizer-BioNTech COVID-19 Vaccine (also known as COMIRNATY®, COVID-19 mRNA, Vaccine BNT162b2 or BNT162) or Pfizer COVID-19 Treatment (also known as PAXLOVID™ (nirmatrelvir tablets; ritonavir tablets)), and you are not part of a clinical trial* for this product, click the link below to submit your information:

Pfizer Safety Reporting Site

*If you are involved in a clinical trial for either product, adverse events should be reported to your coordinating study site.

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FDA Medwatch
You may also contact the U.S. Food and Drug Administration (FDA) directly to report adverse events or product quality concerns either online at www.fda.gov/medwatchor by calling
(800)-332-1088.